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FDA 510(k)

RENTON SUCTION DEVICE U.S. PATENT*4,767,404

K-Number: K962920 · 1996-10-21

ApplicantR&S Surgical, LLC
Decision Date1996-10-21
Product CodeGCX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RENTON SUCTION DEVICE U.S. PATENT*4,767,404 is the device name listed in this FDA 510(k) record. The listed applicant is R&S Surgical, LLC. It received FDA 510(k) clearance on 1996-10-21 under 510(k) number K962920. The device is classified under product code GCX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RENTON SUCTION DEVICE U.S. PATENT*4,767,404?

RENTON SUCTION DEVICE U.S. PATENT*4,767,404 is a medical device that received FDA 510(k) clearance on 1996-10-21. The listed applicant is R&S Surgical, LLC. The 510(k) number is K962920.

When did RENTON SUCTION DEVICE U.S. PATENT*4,767,404 receive FDA 510(k) clearance?

RENTON SUCTION DEVICE U.S. PATENT*4,767,404 received FDA 510(k) clearance on 1996-10-21, under 510(k) number K962920.

Who is the listed applicant for RENTON SUCTION DEVICE U.S. PATENT*4,767,404?

The FDA 510(k) record lists R&S Surgical, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RENTON SUCTION DEVICE U.S. PATENT*4,767,404?

The FDA product code for RENTON SUCTION DEVICE U.S. PATENT*4,767,404 is GCX.

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Related Devices (Code: GCX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K042454STRYKER CASSETTE PUMPStryker EndoscopyK992126CIRCON SURGIFLEX WAVE TSUNAMI SUCTION-IRRIGATION SYSTEMCircon Corp.K972074SUCTION INSTRUMENTATIONWalter Lorenz Surgical, Inc.K971022CHASE SUCKERChase Medical, Inc.K964127MEDI-VAC FLEXI-CLEAR SUCTION HANDLEAllegiance Healthcare Corp.K964519CURITY THORACENTESIS TRAYKendall Healthcare Products Co. Div.Of Tyco Health

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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